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Peripheral Blood Vessel Support Frame - Vietnam Registration 2402837ĐKLH/BYT-HTTB

Access comprehensive regulatory information for Peripheral Blood Vessel Support Frame in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại D medical device is registered under number 2402837ĐKLH/BYT-HTTB and manufactured by Angiomed GmbH & Co. Medizintechnik KG. The authorized representative in Vietnam is CÔNG TY TNHH DK MEDICAL.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.

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2402837ĐKLH/BYT-HTTB
Registration Details
Vietnam MOH Registration: 2402837ĐKLH/BYT-HTTB
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Device Details

Peripheral Blood Vessel Support Frame
VN: Khung giá đỡ mạch máu ngoại vi
Risk Class TTBYT Loại D

Registration Details

2402837ĐKLH/BYT-HTTB

000.00.04.G18-220329-0024

Theo theo phụ lục

Theo phụ lục

Company Information

Theo theo phụ lục

Angiomed GmbH & Co. Medizintechnik KG

Technical Details

E-Luminexx™ stent is indicated for the treatment of atherosclerotic lesions in the common iliac artery and the external iliac artery

Dates and Status

Oct 22, 2024